Newly synthesized oleylgingerol and oleylshogaol activate TRPV1 ion channels

Biosci Biotechnol Biochem. 2007 Sep;71(9):2304-7. doi: 10.1271/bbb.70187. Epub 2007 Sep 7.

Abstract

The oleyl moiety in vanilloids is important in activating vanilloid receptor 1 (TRPV1), but there was no ingredient of ginger containing the oleyl moiety in the natural form. We synthesized oleylgingerol and oleylshogaol and then evaluated their potential to activate a rat TRPV1 channel. Oleylgingerol is a stronger TRPV1 agonist than natural gingerols, but oleylshogaol is a weaker agonist than natural shogaols. The difference in structure between oleylgingerol and oleylshogaol is only the hydroxy group at carbon-5. This hydroxy group might have an important role in activating a TRPV1 channel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism
  • Cell Line
  • Fatty Alcohols / chemical synthesis*
  • Fatty Alcohols / chemistry
  • Fatty Alcohols / pharmacology*
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Kidney / drug effects
  • Kidney / metabolism
  • Molecular Structure
  • Rats
  • Structure-Activity Relationship
  • TRPV Cation Channels / metabolism*

Substances

  • Fatty Alcohols
  • TRPV Cation Channels
  • Trpv1 protein, rat
  • oleylgingerol
  • oleylshogaol
  • Calcium